Li Y, Guo Y, Cao F, Guo S, Xue D, Zhou Z, Hao X, Tong L, Fu Q
Department of Anesthesia, First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
Department of Anesthesia, 71st Group Army Hospital of CPLA Army, Xuzhou 221004, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Mar 20;44(3):420-427. doi: 10.12122/j.issn.1673-4254.2024.03.02.
To investigate the role of glutamatergic neurons in the dorsomedial periaqueductal grey (dmPAG) in regulating excessive defensive behaviors in mice with post-traumatic stress disorder (PTSD).
Eight-week-old male C57BL/6 mice were subjected to stereotactic injections of different recombinant adeno- associated viral vectors (rAAV2/9-CaMKII-mCherry, rAAV2/9-CaMKII-hM3Dq-mCherry and rAAV2/9-CaMKII-hM4Di-mCherry) into the bilateral dmPAG for chemogenetic activation or inhibition of the glutamatergic neurons, followed 2 weeks later by PTSD modeling by single prolonged stress. The looming test, response to whisker stimulation test and contextual fear conditioning (CFC) test were used to observe changes in defensive behaviors of the PTSD mice. The activity of glutamatergic neurons in the dmPAG were observed using immunofluorescence staining.
Compared with the control mice, the mouse models of PTSD showed a shortened latency of flights with increased time spent in the nest, response scores of defensive behaviors and freezing time (all <0.01). Immunofluorescence staining revealed significantly increased c-fos-positive glutamatergic neurons in the dmPAG of PTSD mice with defensive behaviors. Activation of the glutamatergic neurons in the dmPAG (in PTSD hM3Dq group) did not cause significant changes in the latency of flights or time in nest but obviously increased response scores of defensive behaviors and freezing time of the mice, whereas inhibiting the glutamatergic neurons in the dmPAG (in PTSD hM4Di group) caused the reverse changes and obviously alleviated defensive behaviors in the PTSD mice (<0.05 or 0.01).
Inhibiting the activity of glutamatergic neurons in the dmPAG can alleviate defensive behaviors in mice with PTSD.
探讨导水管周围灰质背内侧(dmPAG)中的谷氨酸能神经元在调节创伤后应激障碍(PTSD)小鼠过度防御行为中的作用。
对8周龄雄性C57BL/6小鼠进行立体定向注射不同的重组腺相关病毒载体(rAAV2/9-CaMKII-mCherry、rAAV2/9-CaMKII-hM3Dq-mCherry和rAAV2/9-CaMKII-hM4Di-mCherry)至双侧dmPAG,以化学遗传学方式激活或抑制谷氨酸能神经元,2周后通过单次长时间应激进行PTSD建模。采用逼近试验、对触须刺激的反应试验和情境恐惧条件化(CFC)试验观察PTSD小鼠防御行为的变化。通过免疫荧光染色观察dmPAG中谷氨酸能神经元的活性。
与对照小鼠相比,PTSD小鼠模型的飞行潜伏期缩短,在巢内停留时间、防御行为反应评分和僵住时间增加(均P<0.01)。免疫荧光染色显示,出现防御行为的PTSD小鼠dmPAG中c-fos阳性谷氨酸能神经元显著增加。激活dmPAG中的谷氨酸能神经元(PTSD hM3Dq组)未引起飞行潜伏期或巢内停留时间的显著变化,但明显增加了小鼠的防御行为反应评分和僵住时间,而抑制dmPAG中的谷氨酸能神经元(PTSD hM4Di组)则产生相反的变化,并明显减轻了PTSD小鼠的防御行为(P<0.05或P<0.01)。
抑制dmPAG中谷氨酸能神经元的活性可减轻PTSD小鼠的防御行为。